N-18 (KOLFOCON A),N-32 (KOLFOCON B) LENS MATERIAL

FDA Premarket Approval P880024 S003

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

DeviceN-18 (KOLFOCON A),N-32 (KOLFOCON B) LENS MATERIAL
Generic NameLens, Contact (other Material) - Daily
ApplicantTHE LAGADO CORP.
Date Received1993-03-05
Decision Date1994-03-04
PMAP880024
SupplementS003
Product CodeHQD 
Advisory CommitteeOphthalmic
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address THE LAGADO CORP. 2890 South Tejon St. englewood, CO 80110

Supplemental Filings

Supplement NumberDateSupplement Type
P880024Original Filing
S003 1993-03-05 Normal 180 Day Track
S002 1993-03-05 Normal 180 Day Track
S001

NIH GUDID Devices

Device IDPMASupp
00858174006027 P880024 002
00858174006010 P880024 002

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